Could a simple checklist make hospital discharge safer and more satisfying for surgery patients?
NCT ID NCT07713147
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study tests whether a patient safety checklist (PASC) helps adults recovering from major surgery feel more satisfied with their discharge education and reduces communication problems with healthcare staff. About 264 participants will either use the checklist from the day surgery is scheduled until discharge or receive standard care. The goal is to see if a simple tool can improve how well patients understand their recovery plan and feel heard.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a patient safety checklist for self-use during the perioperative period
- What this could lead to
- If effective, this simple checklist could improve how well surgical patients understand their discharge instructions and feel heard by their healthcare team.
- What could go wrong
- This is a relatively small, single-center trial, and the checklist's benefits may not apply to all hospitals or patient groups. It relies on patients using the checklist correctly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 264 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Willing to participate in the study. * Scheduled to undergo elective primary major surgery. * Aged 18 years or older. * Undergoing a surgical procedure classified as a Category A, B, C, or D (major surgery) according to the Interventional Procedures List of the Turkish Ministry of Health. * Able to understand and complete the checklist, with adequate cognitive ability and no impairment that would interfere with participation. * Able to provide written informed consent in Turkish. Exclusion Criteria: * Undergoing a surgical procedure classified as Category E according to the Interventional Procedures List published by the Turkish Public Hospitals Institution. * Belonging to vulnerable groups, including individuals who are legally restricted, prisoners, or residents of nursing homes. * Being scheduled for day surgery.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Ondokuz Mayıs University Health Practice and Research Center
Samsun, Atakum, 55100, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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